Canonical Allele Identifier: CA269293946

Gene: SPRED1

Linked Data

• dbSNP Id: rs141044168
• gnomAD v3: 15-38356431-C-G
• gnomAD v4: 15-38356431-C-G
• MyVariant Identifiers: chr15:g.38648632C>G (hg19) ; chr15:g.38356431C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38356431C>G , CM000677.2:g.38356431C>G	GRCh38
NC_000015.9:g.38648632C>G , CM000677.1:g.38648632C>G	GRCh37
NC_000015.8:g.36435924C>G	NCBI36
NG_008980.1:g.108581C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.*4767C>G MANE Select	ENSP00000299084.4:n.*4767C>G
ENST00000299084.8:c.*4767C>G	ENSP00000299084.4:n.*4767C>G
NM_152594.2:c.*4767C>G	NP_689807.1:n.*4767C>G
XM_005254202.2:c.*4767C>G	XP_005254259.1:n.*4767C>G
XM_005254203.3:c.*4767C>G	XP_005254260.1:n.*4767C>G
XM_011521288.1:c.*4767C>G	XP_011519590.1:n.*4767C>G
XM_011521289.1:c.*4767C>G	XP_011519591.1:n.*4767C>G
XM_011521290.1:c.*4767C>G	XP_011519592.1:n.*4767C>G
XM_005254202.3:c.*4767C>G	XP_005254259.1:n.*4767C>G
XM_011521289.3:c.*4767C>G	XP_011519591.1:n.*4767C>G
NM_152594.3:c.*4767C>G MANE Select	NP_689807.1:n.*4767C>G